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Influencia*del*lince*ibérico*(Lynx%pardinus)*
en*la*actividad*circadiana*del*zorro*(Vulpes vulpes)
Antón*Álvarez*Bermúdez1,*Germán*Garrote*Alonso1,*Ramón*Perez de*Ayala2
1.-
Instituto*de*Biología*de*la*Conservación*(IBiCo)*-
C/Nebli,*nº*13,*28230,*Madrid
2.-
WWF
-C/*Gran Vía de*San*Francisco,*nº*8,*28005,*Madrid
INTRODUCCIÓN
Actividad%circadiana
Preferencia%temporal
Relación%circadiana%
depredador-presa
Mardia-Watson-Wheeler
+,-./0/012,31-45360/312512/6,31780749/0531
Estimación%de%los%patrones%de%actividad%circadiana
:;436531<,1./0/-=6087,31251>4<78,<53125125<382/21251?50<59
RESULTADOS
Agradecimientos
@36428, 05/98A/2, 5< 59 -/07, 259 .0,B576,
C+,-.565<78/ 8<650!53.57D>87/ B 7,5E8365<78/ 5<605 59
98<75 8F=087, GLynx pardinusH B ,60,3 7/0<DI,0,3J 7,<
59 /.,B, 25 9/ Fundación Barcelona Zoo B59
Ayuntamiento de Barcelona#
::9>,<3, K,05<, L5M/) 6=7<87, 25 7/-., 25 NNO#
** -4B 38M<8>87/68I, *38M<8>87/68I, P-/0M8</9-5<65 38M<8>87/68I,
O8<7/1Q5R/9/;,)1$$%"1S/#15<1T8500/1K,05</1U085<6/9
CS%=%0,30
G")$'!")V'H
CS%=%0,45
G")WV!")&&H
:6/025750:-/<5750
No%Lince
Lince
No%Lince Lince
No%Lince%%%%%%%%%%%Lince
Índice%de%Selección%de%Jacobs
'
MATERIALES YMÉTODOS
Q05>505<78/12591A,00,1.,017/2/1.508,2,128/08,
Coeficiente%solapamiento
X5.0535<6/78Y<125917,5>8785<6512513,9/./-85<6,17807/28/<,
Z,0/
Z,0/
[5<382/21251/768I82/2 [5<382/21251/768I82/2
@9 A,00, reduce el solapamiento
circadiano GWH B 35 .0,2475 4</
sincronización negativa GVH 7,< 59
7,<5;, 25F82, /9/ 8<>945<78/ 259
98<75 8F=087,#
Análisis%estadístico
Lince%VS%%%%%%%%%No%lince
Influencia%del%lince%ibérico
Preferencia%temporal
N\14)55
p= 0)10P
[8>505<78/315<19/1/768I82/217807/28/</125917,<5;,1B1
591A,00,125F82,1/19/18<>945<78/1259198<7518F=087,
N\12)79
p= 0)41
@< 59 /;4365 25 9/ /768I82/2 7807/28/</ 259
A,00, 7,-, -57/<83-, 25 7,5E8365<78/
7,< 59 98<75 8F=087, ,F65<5-,3 I/9,053
-/0M8</9-5<65 38M<8>87/68I,3 G'H#
@9 A,00, aumenta su actividad nocturna B
reduce su actividad diurna 25F82, /9/
8<>945<78/ 259 98<75 8F=087, G$H#
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"!
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No%Lince Lince
Grado%de%sincronización
Ø]-.,06/<78/ 25 9/ 28-5<38Y< 65-.,0/9 circadiana 5< 59 536428, 25 9/ relación entre el zorro yel lince ibérico.
Ø^/ .9/368782/2 259 A,00, 95 .50-865 05/98A/0 4< trade-off 5<605_
ØT/683>/750 343 05`4508-85<6,3 Fa387,3 G>4<2/-5<6/9-5<65 59 /7753, /9 7,<5;,H#
Ø+,365 25 4</ .,38F95 -45065 .05-/640/ 25F82/ /9 5<745<60, 7,< 4< 98<75 8F=087,#
Lince%ibérico
+,-.5682,0134.508,0b%c
+,<60,9/2,01</640/9125111111111111111111111111
25.052/2,053
Zorro
Especie%subordinadab%c #
%"!ddebfc Conejo%%%gd"e
:96,13,9/./-85<6,160Y>87,1
Q08<78./91modulador 2519,31./60,<531251
/768I82/217807/28/</1251/-F/3153.57853bh)dc
K/B,01plasticidad #
5<19,31patrones .
de%actividad%circadiana%%%%%%%.
2519,31-53,7/0<DI,0,318F=087,3b&c .
ØDos especies competidoras 35M05M/< /9, 9/0M, 25 /9M4</ 28-5<38Y< 25 34 <87S, 57,9YM87,
G53./78/9) 60Y>87/) Btemporalb'cH./0/ .,250 7,5E83680b$)Wc#
Ø^/3 interacciones intragremiales asimétricas G7,< 4< 7,-.5682,0 34.508,0 B,60, 8<>508,0H
3,< >05745<653 5<605 carnívorosbVc#
Ø^/ especie subordinada G7,-.5682,0 8<>508,0H /;436/ 34 7,-.,06/-85<6, ./0/ -8<8-8A/0 9,3
5<745<60,3 /<6/M,<836/3 7,< 34 7,-.5682,0 34.508,0#
Ø^,3 mesocarnívoros /-5<42, 35M05M/< 5< 343 patrones de actividad circadianob&c#
•'h1536/78,<531251>,6,!60/-.5,1GK/B,ij498,H
7,9,7/2/31/91./3,15<17/-8<,31,1I5052/31B138<1/60/B5<65
Lince ($Vh1<,7S53!60/-./H
[,3198<75318F=087,31058<60,24782,315<1$"'%
No%Lince%($W% <,7S53!60/-./H
Q0535<78/125198<751/<572Y687/
≃SaF86/6
≃]:X17,<5;,
Área%de%estudio
CONCLUSIONES
biologiadelaconservacion.org
1. T7S,5<50)1k#1N#1X53,4075 Q/06868,<8<M 8<1@7,9,M87/9 +,--4<86853#1Science 185, $fiWd1G'dfVH#
2. Z/028<)1l#1kS5 +,-.56868I5 @E79438,< Q08<78.95#1Science 131, '$d$i'$df1G'd%"H#
3. TA/FY)1Q#1m1K53A=</)1l#1^8-868<M 38-89/086B 05I838652#1Oikos 112, %'$i%'d1G$""%H#
4. Q/9,-/053)1O#1m1+/0,)1k#1K#1]<6503.578>87 ?8998<M /-,<M K/--/98/< +/0<8I,053#1The American6Naturalist 153,
Vd$i&"h1G'dddH#
5. K,<6500,3,)1Q#)1:9I53)1Q#1+#1m1O50050/3)1Q#1Q9/368786B 8<17807/28/< /768I86B ./6650<3 ,>1-53,7/0<8I,053 8<1T,46Sn53650<
@40,.5_18-.987/68,<3 >,0 3.57853 7,5E8365<75#1Behavioral Ecology and6Sociobiology 68, 'V"Wi'V'f1G$"'VH#
6.%Q/9,-/053)1O#)1O50050/3)1Q#)1O5208/<8)1j#1K#1m1[598F53)1K#1T./68/9 X59/68,<3S8.3 o56n55< ]F508/< ^B<E1/<21U6S50
+/0<8I,053 8<1/< :05/ ,>1T,46S!N53650<1T./8<#1The Journal of6Applied Ecology 33, &1G'dd%H#
7.%O50</<25A!25!T8-,<)1j#1et6al. +/<1n8253.05/2 M5<50/9836 .052/6,03 />>576 p5B36,<5 .05Bq1:17/3513642B n86S 0521>,E53
/<21@40,.5/< 0/FF863 8<16S580 </68I5 0/<M5#1Population Ecology 57, &d'i&dd1G$"'&H#
8. [D/A!X48A)1O#)1+/0,)1j#)1[598F53!K/65,3)1K#)1:00,B,)1o#1m1O50050/3)1Q#1[08I5031,>10521>,E G1Vulpes vulpes H12/89B /768I86B_1.05B
/I/89/F8986B)1S4-/<1283640F/<75 ,0 S/F86/6 360476405q1Journal of6Zoology 298, '$hi'Wh1G$"'%H#
9. r50M/)1j#1et6al. U<6,M5<B ,>12/89B /768I86B /<217807/28/< 0SB6S- 8<16S5 ]F508/< 9B<E G^B<E1./028<43H#1Applied Animal6
Behaviour Science 169, %$i%h1G$"'&H#
10. O05B)1T#)1O83S50)1j#1k#)1o406,<)1:#1+#1m1L,9.5)1j#1Q#1]<I5368M/68<M /<8-/91/768I86B ./6650<3 /<2165-.,0/91<87S51./06868,<8<M
438<M 7/-50/!60/. 2/6/_17S/995<M53 /<21,..,064<86853#1Remote Sensing in6Ecology and6Conservation G$"'fH#1
11.%K,<6500,3,)1Q#)1:9I53)1Q#1+#1m1O50050/3)1Q#1+/67S1K51]> r,4 +/<_1[859 :768I86B Q/6650<3 ,>1K/--/98/< Q05B /<21Q052/6,03#1
Ethology 119, '"VVi'"&%1G$"'WH#
¿La%presencia%del%lince%ibérico%afecta%a%los%patrones%de%actividad%circadiana%del%zorro?
¿La%relación%circadiana%del%zorro%con%el%conejo%es%alterada%por%la%presencia%del%lince%ibérico?
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Relación%circadiana%depredador-presa
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Índice%de%Selección%de%Jacobs
Q05>505<78/1.,017/2/1.508,2,125912D/b&c
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Coeficiente%de%solapamiento
Q05>505<78/1.,017/2/1.508,2,125912D/
W
Grado%de%sincronización
@368-/2,1-528/<6517,0059/78,<531251Q5/03,<
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Bibliografía
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